US8551894B2ActiveUtilityPatentIndex 89
Ligand graft functionalized substrates
Est. expirySep 19, 2028(~2.2 yrs left)· nominal 20-yr term from priority
Y10T428/249991Y10T428/249978Y10T442/2033Y10T428/2935C08J 2327/14B01D 39/1676C07K 1/34Y10T442/2525Y10T442/60C08J 7/18
89
PatentIndex Score
20
Cited by
98
References
17
Claims
Abstract
Polyethyleneimine and polyalkylene biguanide ligand functionalized substrates, methods of making ligand functionalized substrates, and methods of using functionalized substrates are disclosed.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1. An article comprising a porous thermoplastic substrate and extending from the surfaces thereof free-radically grafted biguanide ligand groups to form a free-radically-grafted substrate, wherein the free-radically grafted substrate is of the formula: Substrate˜(M ligand ) m , where Substrate represents the thermoplastic substrate, M ligand represents a polymerized grafted ethylenically unsaturated monomer having pendant biguanide ligand groups, and m is at least two;
wherein said pendent biguanide ligands groups are selected from one or more of the formula:
wherein
R 2 is an arylene or alkylene and a is at least one and wherein the grafted ligand groups comprise the reaction product of a free-radically grafted electrophilic functional group and a ligand compound:
wherein
each R 4 is individually H, alkyl or aryl,
each R 6 is individually alkylene or arylene,
c may be zero or an integer from 1 to 500, and
d is zero or 1, with the proviso that when d is zero, then c is 1 to 500.
2. The article of claim 1 , further comprising free-radically grafted quaternary ammonium groups on the surface of the substrate.
3. The article of claim 1 , wherein the porous substrate is selected from a porous membrane, porous non-woven web, or porous fiber.
4. The article of claim 1 , wherein the grafted biguanide ligand groups comprise the reaction product of (a) a first free-radically grafted electrophilic functional group comprising an epoxy group, an isocyanato group, or an azlactone group with (b) a ligand compound:
wherein
each R 4 is individually H, alkyl or aryl,
each R 6 is individually alkylene or arylene,
c may be zero or an integer from 1 to 500, and
d is zero or 1, with the proviso that when d is zero, then c is 1 to 500.
5. An article of claim 1 comprising a porous base substrate having interstitial and outer surfaces; and grafted ligand groups extending from the surfaces of the porous base substrate, wherein the grafted ligand groups comprise the reaction product of a free-radically grafted electrophilic functional group and a ligand compound:
wherein
each R 4 is individually H, alkyl or aryl,
each R 6 is individually alkylene or arylene,
c may be zero or an integer from 1 to 500, and
d is zero or 1, with the proviso that when d is zero, then c is 1 to 500.
6. The article of claim 5 , wherein the free-radically grafted electrophilic functional group is selected from (i) an epoxy group or a ring-opened epoxy linkage group, (ii) an azlactone group or a ring-opened azlactone linkage group, or (iii) an isocyanato group.
7. The article of claim 5 , further comprising free-radically grafted ionic or hydrophilic groups.
8. The article of claim 7 , wherein the free-radically grafted ionic groups are grafted quaternary ammonium groups.
9. The article of claim 5 , wherein the porous base substrate is microporous.
10. The article of claim 5 , wherein the article further comprises free-radically grafted hydrophilic groups.
11. The article of claim 5 , wherein the porous base substrate comprises a porous membrane, a porous nonwoven web, or a porous fiber.
12. The article of claim 5 , wherein the free-radically grafted ligand groups comprise the reaction product of (a) a first grafted electrophilic functional group comprising an epoxy group, an isocyanato group, or an azlactone group with (b) a ligand compound:
wherein
each R 4 is individually H, alkyl or aryl,
each R 6 is individually alkylene or arylene,
c may be zero or an integer from 1 to 500, and
d is zero or 1, with the proviso that when d is zero, then c is 1 to 500.
13. A method of preparing a ligand functional substrate of claim 1 comprising:
1) providing a thermoplastic polymer substrate;
2) free-radically grafting a functional group to the surface of the substrate to produce a substrate having a grafted electrophilic functional groups extending from the surface(s) thereof; and
3) reacting the grafted electrophilic functional groups with biguanide ligand groups to produce a substrate having grafted biguanide ligand groups extending from the surface(s) of the substrate.
14. The method of claim 13 , comprising the steps of:
a) providing a porous thermoplastic polymer base substrate;
b) imbibing the porous thermoplastic polymer base substrate with a first solution to form an imbibed porous base substrate, the first solution comprising at least one grafting monomer having (a) a free-radically polymerizable group and (b) an additional electrophilic functional group;
c) exposing the imbibed porous base substrate to a controlled amount of electron beam radiation so as to form a first functionalized substrate having free-radically grafted electrophilic functional groups;
d) reacting the functionalized substrate having grafted electrophilic functional groups with a ligand compound:
wherein
each R 4 is individually H, alkyl or aryl,
each R 6 is individually alkylene or arylene,
c may be zero or an integer from 1 to 500, and
d is zero or 1, with the proviso that when d is zero, then c is 1 to 500.
15. The method of claim 14 , wherein the imbibing solution further comprises a second grafting monomer having (a) a free-radically polymerizable group and (b) an ionic group or a hydrophilic group.
16. The method of claim 15 , further comprising the steps of:
imbibing the first functionalized substrate with a second solution to form a first imbibed functionalized substrate, the second solution comprising at second grafting monomer having (a) a free-radically polymerizable group and (b) a second quaternary ammonium group, and
exposing the first imbibed functionalized substrate to a controlled amount of electron beam radiation so as to form a second functionalized substrate comprising free-radically grafted quaternary ammonium groups attached to the surfaces of the porous base substrate.
17. The method of claim 13 , wherein the biguanide ligand groups are one or more of the formula:
wherein
R 2 is an arylene or alkylene and a is at least one.Cited by (0)
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